Canonical Allele Identifier: CA2642410989
Gene: CYP4F22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529699C>T , CM000681.2:g.15529699C>T GRCh38
NC_000019.9:g.15640510C>T , CM000681.1:g.15640510C>T GRCh37
NC_000019.8:g.15501510C>T NCBI36
NG_007987.1:g.26175C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.223-10C>T MANE Select ENSP00000269703.1:n.223-10C>T
ENST00000269703.7:c.223-10C>T ENSP00000269703.1:n.223-10C>T
ENST00000601005.2:c.223-10C>T ENSP00000469866.1:n.223-10C>T
NM_173483.3:c.223-10C>T NP_775754.2:n.223-10C>T
XM_011527692.1:c.223-10C>T XP_011525994.1:n.223-10C>T
XM_011527693.1:c.223-10C>T XP_011525995.1:n.223-10C>T
XM_011527692.2:c.223-10C>T XP_011525994.1:n.223-10C>T
XM_011527693.2:c.223-10C>T XP_011525995.1:n.223-10C>T
NM_173483.4:c.223-10C>T MANE Select NP_775754.2:n.223-10C>T